| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g18070 | A02 | 9087144 | G | A | missense_variant | MODERATE | c.1766C>T|p.Ser589Phe |
S133 |
| 2 | BAA02g18070 | A02 | 9087771 | G | A | missense_variant | MODERATE | c.1139C>T|p.Ala380Val |
S4 |
| 3 | BAA02g18070 | A02 | 9088138 | C | T | missense_variant | MODERATE | c.772G>A|p.Val258Ile |
S186 |
| 4 | BAA02g18070 | A02 | 9088599 | G | A | synonymous_variant | LOW | c.391C>T|p.Leu131Leu |
S70 |
| 5 | BAA02g18070 | A02 | 9088976 | C | T | synonymous_variant | LOW | c.213G>A|p.Lys71Lys |
S196 |
| 6 | BAA02g18070 | A02 | 9089520 | C | T | upstream_gene_variant | MODIFIER | c.-332G>A| |
S124 |
| 7 | BAA02g18070 | A02 | 9089733 | C | T | upstream_gene_variant | MODIFIER | c.-545G>A| |
S233 |
| 8 | BAA02g18070 | A02 | 9091404 | G | A | upstream_gene_variant | MODIFIER | c.-2216C>T| |
S168 |
| 9 | BAA02g18070 | A02 | 9093277 | C | T | upstream_gene_variant | MODIFIER | c.-4089G>A| |
S302 |
| 10 | BAA02g18070 | A02 | 9093672 | G | A | upstream_gene_variant | MODIFIER | c.-4484C>T| |
S116 |